Mutagenetix > Incidental Mutation

Incidental Mutation 'R3847:Cul9'

277460

Institutional Source

Beutler Lab

Gene Symbol

Cul9

Ensembl Gene

ENSMUSG00000040327

Gene Name

cullin 9

Synonyms

1810035I07Rik, Parc

MMRRC Submission

040895-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.294) question?

Stock #

R3847 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

46500572-46546388 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 46525135 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 1195 (Y1195C)

Ref Sequence

ENSEMBL: ENSMUSP00000138418 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000066026] [ENSMUST00000182485]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000066026
AA Change: Y1195C

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000067736
Gene: ENSMUSG00000040327
AA Change: Y1195C

Domain	Start	End	E-Value	Type
low complexity region	46	61	N/A	INTRINSIC
low complexity region	119	131	N/A	INTRINSIC
low complexity region	345	357	N/A	INTRINSIC
Pfam:Cul7	367	441	1e-35	PFAM
low complexity region	447	460	N/A	INTRINSIC
low complexity region	525	540	N/A	INTRINSIC
low complexity region	845	860	N/A	INTRINSIC
low complexity region	873	880	N/A	INTRINSIC
APC10	1166	1325	1.97e-56	SMART
low complexity region	1437	1450	N/A	INTRINSIC
low complexity region	1563	1578	N/A	INTRINSIC
low complexity region	1646	1671	N/A	INTRINSIC
Cullin_Nedd8	1867	1950	7.55e-6	SMART
Blast:RING	2074	2122	2e-13	BLAST
IBR	2144	2207	8.99e-14	SMART
IBR	2228	2283	4.66e-2	SMART
low complexity region	2503	2520	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181301

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182315

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182451

Predicted Effect

probably damaging
Transcript: ENSMUST00000182485
AA Change: Y1195C

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000138418
Gene: ENSMUSG00000040327
AA Change: Y1195C

Domain	Start	End	E-Value	Type
low complexity region	46	61	N/A	INTRINSIC
low complexity region	119	131	N/A	INTRINSIC
low complexity region	345	357	N/A	INTRINSIC
Pfam:Cul7	367	442	1.4e-33	PFAM
low complexity region	447	460	N/A	INTRINSIC
low complexity region	525	540	N/A	INTRINSIC
low complexity region	845	860	N/A	INTRINSIC
low complexity region	873	880	N/A	INTRINSIC
APC10	1166	1325	1.97e-56	SMART
low complexity region	1437	1450	N/A	INTRINSIC
low complexity region	1563	1578	N/A	INTRINSIC
low complexity region	1646	1671	N/A	INTRINSIC
Cullin_Nedd8	1867	1950	7.55e-6	SMART
Blast:RING	2074	2122	3e-13	BLAST
IBR	2144	2207	8.99e-14	SMART
IBR	2228	2283	4.66e-2	SMART
coiled coil region	2461	2497	N/A	INTRINSIC
low complexity region	2513	2530	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182530

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182668

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182799

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183016

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183078

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183163

Meta Mutation Damage Score

0.6024

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.7%
20x: 96.1%

Validation Efficiency

100% (66/66)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased body weight, increased incidence of tumors, and decreased cellular sensitivity to radiation-induced apoptosis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930522L14Rik	T	C	5: 109,736,324 (GRCm38)		probably null	Het
Abcc12	C	T	8: 86,553,391 (GRCm38)	E338K	probably benign	Het
Abcc5	A	T	16: 20,372,156 (GRCm38)	S815T	probably benign	Het
Ankrd16	G	A	2: 11,789,808 (GRCm38)	E335K	probably benign	Het
Atm	A	G	9: 53,503,075 (GRCm38)	F905S	possibly damaging	Het
Bckdha	C	T	7: 25,631,652 (GRCm38)	R281H	probably damaging	Het
Blvra	C	T	2: 127,095,191 (GRCm38)	T188I	probably damaging	Het
Bmp8b	C	A	4: 123,116,168 (GRCm38)		probably benign	Het
Cacna2d3	A	G	14: 29,347,120 (GRCm38)		probably null	Het
Cacng8	T	C	7: 3,394,474 (GRCm38)	S84P	probably damaging	Het
Cad	T	A	5: 31,061,650 (GRCm38)	V605E	probably damaging	Het
Ccny	A	G	18: 9,449,641 (GRCm38)	S11P	probably benign	Het
Col3a1	C	A	1: 45,321,990 (GRCm38)	P112T	unknown	Het
Corin	T	C	5: 72,422,165 (GRCm38)	E155G	probably benign	Het
Cyp27a1	A	G	1: 74,737,559 (GRCm38)	E501G	probably damaging	Het
Dennd3	T	A	15: 73,542,732 (GRCm38)	N457K	possibly damaging	Het
Dnah7a	T	G	1: 53,501,656 (GRCm38)	I2520L	probably benign	Het
Dst	C	T	1: 34,212,319 (GRCm38)	S4165F	probably damaging	Het
Fgf14	A	C	14: 123,980,389 (GRCm38)	I234R	probably benign	Het
Foxp4	A	G	17: 47,875,528 (GRCm38)	I442T	unknown	Het
Gad2	T	G	2: 22,684,988 (GRCm38)	D472E	probably benign	Het
Garnl3	G	T	2: 32,992,228 (GRCm38)	H832N	probably benign	Het
Gm13941	T	C	2: 111,104,853 (GRCm38)	M11V	unknown	Het
Gnptab	T	A	10: 88,433,577 (GRCm38)	L714*	probably null	Het
Golgb1	C	A	16: 36,898,733 (GRCm38)	Q334K	probably benign	Het
Gp9	A	G	6: 87,779,151 (GRCm38)	I49M	probably benign	Het
Guf1	A	G	5: 69,561,157 (GRCm38)	N213S	probably damaging	Het
H2-K1	T	G	17: 33,997,329 (GRCm38)	H281P	probably damaging	Het
Hhip	T	A	8: 79,997,495 (GRCm38)	M373L	probably benign	Het
Ifi203	C	T	1: 173,933,796 (GRCm38)	C229Y	possibly damaging	Het
Ighv13-2	A	G	12: 114,357,798 (GRCm38)	L88S	probably damaging	Het
Kcna3	T	C	3: 107,036,696 (GRCm38)	Y92H	possibly damaging	Het
Lmo7	A	G	14: 101,922,095 (GRCm38)		probably null	Het
Lrguk	A	G	6: 34,073,768 (GRCm38)	D387G	probably damaging	Het
Mki67	A	C	7: 135,696,130 (GRCm38)	S2392A	probably benign	Het
Mknk2	C	T	10: 80,667,975 (GRCm38)	W367*	probably null	Het
Mocos	A	G	18: 24,676,662 (GRCm38)	K441E	probably damaging	Het
Mpnd	T	C	17: 56,011,692 (GRCm38)	S150P	probably damaging	Het
Naip2	A	T	13: 100,179,432 (GRCm38)	L280Q	probably damaging	Het
Naip2	G	C	13: 100,179,433 (GRCm38)	L280V	probably damaging	Het
Neurod4	C	T	10: 130,270,482 (GRCm38)	V308I	probably benign	Het
Nxf3	C	T	X: 136,073,983 (GRCm38)	V474I	probably benign	Het
Or10d5j	A	T	9: 39,956,581 (GRCm38)	M118K	probably damaging	Het
Or8u10	A	T	2: 86,085,407 (GRCm38)	Y123*	probably null	Het
Pam	T	A	1: 97,854,756 (GRCm38)		probably benign	Het
Pde5a	T	C	3: 122,803,160 (GRCm38)	Y467H	probably damaging	Het
Pibf1	T	A	14: 99,137,121 (GRCm38)	V332E	possibly damaging	Het
Plxna1	C	A	6: 89,356,519 (GRCm38)	R376L	probably damaging	Het
Proz	A	G	8: 13,073,533 (GRCm38)	E268G	probably benign	Het
Rimbp3	A	T	16: 17,210,299 (GRCm38)	H529L	probably benign	Het
Rnf103	C	G	6: 71,508,875 (GRCm38)	C163W	probably damaging	Het
Rnf17	T	C	14: 56,512,296 (GRCm38)	V1433A	probably damaging	Het
Septin11	G	T	5: 93,162,167 (GRCm38)	M276I	probably damaging	Het
Slc30a4	A	G	2: 122,702,272 (GRCm38)	V50A	probably damaging	Het
Sorbs1	A	G	19: 40,314,443 (GRCm38)	V570A	probably damaging	Het
Spout1	T	C	2: 30,177,407 (GRCm38)		probably null	Het
Syne2	T	C	12: 76,048,622 (GRCm38)	L5241P	probably damaging	Het
Tas2r110	T	A	6: 132,868,675 (GRCm38)	I223N	probably damaging	Het
Tead2	T	A	7: 45,232,328 (GRCm38)		probably null	Het
Thsd1	A	G	8: 22,259,411 (GRCm38)	H713R	probably damaging	Het
Ttc21b	A	G	2: 66,242,679 (GRCm38)	L221S	probably damaging	Het
Ugcg	C	T	4: 59,207,798 (GRCm38)	P46S	probably benign	Het
Vmn2r105	A	G	17: 20,208,690 (GRCm38)	I708T	possibly damaging	Het
Vmn2r117	G	T	17: 23,460,415 (GRCm38)	H612N	probably damaging	Het
Wnk1	C	T	6: 119,969,354 (GRCm38)	G613S	possibly damaging	Het
Zbtb41	T	A	1: 139,423,996 (GRCm38)	H282Q	probably benign	Het
Zfp335	C	A	2: 164,900,106 (GRCm38)		probably null	Het
Zmym2	T	A	14: 56,921,499 (GRCm38)		probably benign	Het

Other mutations in Cul9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00087:Cul9	APN	17	46,525,709 (GRCm38)	missense	probably damaging	1.00
IGL00330:Cul9	APN	17	46,510,841 (GRCm38)	splice site	probably benign
IGL00726:Cul9	APN	17	46,528,096 (GRCm38)	missense	probably damaging	1.00
IGL01020:Cul9	APN	17	46,539,023 (GRCm38)	missense	probably damaging	1.00
IGL01358:Cul9	APN	17	46,538,314 (GRCm38)	missense	probably damaging	1.00
IGL01410:Cul9	APN	17	46,528,646 (GRCm38)	missense	probably damaging	0.99
IGL01781:Cul9	APN	17	46,539,304 (GRCm38)	missense	probably benign
IGL01873:Cul9	APN	17	46,502,452 (GRCm38)	missense	probably damaging	0.99
IGL02117:Cul9	APN	17	46,540,375 (GRCm38)	missense	probably benign	0.00
IGL02300:Cul9	APN	17	46,521,032 (GRCm38)	splice site	probably benign
IGL02426:Cul9	APN	17	46,523,258 (GRCm38)	missense	possibly damaging	0.95
IGL02427:Cul9	APN	17	46,502,632 (GRCm38)	missense	possibly damaging	0.69
IGL02496:Cul9	APN	17	46,540,376 (GRCm38)	missense	possibly damaging	0.72
IGL03008:Cul9	APN	17	46,502,697 (GRCm38)	splice site	probably benign
IGL03059:Cul9	APN	17	46,538,987 (GRCm38)	missense	probably damaging	0.98
IGL03302:Cul9	APN	17	46,526,640 (GRCm38)	missense	probably damaging	0.98
bottlenose	UTSW	17	46,500,844 (GRCm38)	missense	possibly damaging	0.79
flipper	UTSW	17	46,525,892 (GRCm38)	missense	probably benign	0.05
orca	UTSW	17	46,525,135 (GRCm38)	missense	probably damaging	1.00
FR4340:Cul9	UTSW	17	46,500,853 (GRCm38)	small insertion	probably benign
FR4449:Cul9	UTSW	17	46,500,856 (GRCm38)	small insertion	probably benign
FR4737:Cul9	UTSW	17	46,500,858 (GRCm38)	small insertion	probably benign
FR4737:Cul9	UTSW	17	46,500,846 (GRCm38)	small insertion	probably benign
FR4976:Cul9	UTSW	17	46,500,853 (GRCm38)	small insertion	probably benign
FR4976:Cul9	UTSW	17	46,500,850 (GRCm38)	small insertion	probably benign
FR4976:Cul9	UTSW	17	46,500,848 (GRCm38)	small insertion	probably benign
FR4976:Cul9	UTSW	17	46,500,856 (GRCm38)	small insertion	probably benign
R0012:Cul9	UTSW	17	46,538,510 (GRCm38)	missense	probably benign	0.26
R0079:Cul9	UTSW	17	46,537,663 (GRCm38)	nonsense	probably null
R0143:Cul9	UTSW	17	46,526,410 (GRCm38)	missense	possibly damaging	0.65
R0390:Cul9	UTSW	17	46,528,589 (GRCm38)	missense	probably benign	0.34
R0401:Cul9	UTSW	17	46,541,704 (GRCm38)	missense	probably damaging	1.00
R0529:Cul9	UTSW	17	46,520,468 (GRCm38)	splice site	probably benign
R0815:Cul9	UTSW	17	46,537,822 (GRCm38)	splice site	probably null
R0863:Cul9	UTSW	17	46,537,822 (GRCm38)	splice site	probably null
R0972:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1173:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1216:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1217:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1261:Cul9	UTSW	17	46,525,782 (GRCm38)	missense	probably damaging	1.00
R1278:Cul9	UTSW	17	46,500,849 (GRCm38)	small deletion	probably benign
R1281:Cul9	UTSW	17	46,511,534 (GRCm38)	missense	probably damaging	1.00
R1349:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1372:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1403:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1403:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1405:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1405:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R1467:Cul9	UTSW	17	46,525,373 (GRCm38)	missense	probably damaging	1.00
R1467:Cul9	UTSW	17	46,525,373 (GRCm38)	missense	probably damaging	1.00
R1482:Cul9	UTSW	17	46,508,547 (GRCm38)	missense	probably damaging	0.99
R1491:Cul9	UTSW	17	46,538,564 (GRCm38)	nonsense	probably null
R1618:Cul9	UTSW	17	46,525,892 (GRCm38)	missense	probably benign	0.05
R1641:Cul9	UTSW	17	46,543,560 (GRCm38)	missense	possibly damaging	0.96
R1679:Cul9	UTSW	17	46,521,156 (GRCm38)	missense	possibly damaging	0.90
R1771:Cul9	UTSW	17	46,537,812 (GRCm38)	missense	probably benign	0.41
R1803:Cul9	UTSW	17	46,503,097 (GRCm38)	missense	probably damaging	1.00
R2020:Cul9	UTSW	17	46,522,175 (GRCm38)	missense	probably damaging	1.00
R2046:Cul9	UTSW	17	46,543,733 (GRCm38)	missense	probably damaging	1.00
R2056:Cul9	UTSW	17	46,543,372 (GRCm38)	missense	probably benign
R2088:Cul9	UTSW	17	46,526,649 (GRCm38)	missense	probably damaging	1.00
R2415:Cul9	UTSW	17	46,543,438 (GRCm38)	missense	probably benign
R2925:Cul9	UTSW	17	46,510,981 (GRCm38)	missense	probably benign	0.08
R2964:Cul9	UTSW	17	46,502,228 (GRCm38)	missense	probably damaging	0.96
R2965:Cul9	UTSW	17	46,502,228 (GRCm38)	missense	probably damaging	0.96
R3690:Cul9	UTSW	17	46,504,031 (GRCm38)	splice site	probably null
R4437:Cul9	UTSW	17	46,502,159 (GRCm38)	missense	probably damaging	1.00
R4470:Cul9	UTSW	17	46,538,336 (GRCm38)	missense	probably benign	0.00
R4540:Cul9	UTSW	17	46,503,089 (GRCm38)	missense	probably null	0.98
R4555:Cul9	UTSW	17	46,501,829 (GRCm38)	missense	possibly damaging	0.82
R4604:Cul9	UTSW	17	46,530,146 (GRCm38)	missense	probably damaging	0.99
R4646:Cul9	UTSW	17	46,539,017 (GRCm38)	nonsense	probably null
R4799:Cul9	UTSW	17	46,500,844 (GRCm38)	missense	possibly damaging	0.79
R4822:Cul9	UTSW	17	46,530,051 (GRCm38)	missense	probably benign	0.01
R4964:Cul9	UTSW	17	46,538,525 (GRCm38)	missense	probably damaging	1.00
R4965:Cul9	UTSW	17	46,538,525 (GRCm38)	missense	probably damaging	1.00
R5027:Cul9	UTSW	17	46,500,782 (GRCm38)	missense	probably damaging	0.99
R5185:Cul9	UTSW	17	46,525,832 (GRCm38)	missense	possibly damaging	0.95
R5237:Cul9	UTSW	17	46,543,467 (GRCm38)	missense	probably benign	0.00
R5278:Cul9	UTSW	17	46,510,873 (GRCm38)	missense	probably damaging	1.00
R5361:Cul9	UTSW	17	46,500,849 (GRCm38)	small deletion	probably benign
R5455:Cul9	UTSW	17	46,510,846 (GRCm38)	splice site	probably null
R5592:Cul9	UTSW	17	46,520,591 (GRCm38)	missense	probably benign	0.00
R5597:Cul9	UTSW	17	46,502,665 (GRCm38)	missense	possibly damaging	0.56
R5613:Cul9	UTSW	17	46,503,844 (GRCm38)	missense	probably damaging	1.00
R6122:Cul9	UTSW	17	46,521,928 (GRCm38)	missense	possibly damaging	0.72
R6135:Cul9	UTSW	17	46,521,453 (GRCm38)	missense	probably benign
R6352:Cul9	UTSW	17	46,511,315 (GRCm38)	missense	probably benign	0.00
R6376:Cul9	UTSW	17	46,508,563 (GRCm38)	missense	probably damaging	1.00
R6868:Cul9	UTSW	17	46,522,183 (GRCm38)	missense	possibly damaging	0.73
R6898:Cul9	UTSW	17	46,511,026 (GRCm38)	missense	possibly damaging	0.87
R7090:Cul9	UTSW	17	46,500,839 (GRCm38)	missense	probably damaging	0.96
R7193:Cul9	UTSW	17	46,538,497 (GRCm38)	missense	probably damaging	0.98
R7221:Cul9	UTSW	17	46,528,565 (GRCm38)	missense	probably damaging	0.99
R7291:Cul9	UTSW	17	46,540,433 (GRCm38)	missense	probably benign	0.00
R7320:Cul9	UTSW	17	46,510,909 (GRCm38)	missense	possibly damaging	0.80
R7348:Cul9	UTSW	17	46,510,993 (GRCm38)	missense	possibly damaging	0.89
R7463:Cul9	UTSW	17	46,520,476 (GRCm38)	splice site	probably null
R7480:Cul9	UTSW	17	46,537,812 (GRCm38)	missense	probably benign	0.41
R7573:Cul9	UTSW	17	46,519,910 (GRCm38)	missense	probably benign
R7582:Cul9	UTSW	17	46,510,979 (GRCm38)	missense	probably damaging	1.00
R7605:Cul9	UTSW	17	46,541,732 (GRCm38)	missense	probably damaging	0.99
R7684:Cul9	UTSW	17	46,509,889 (GRCm38)	missense	probably damaging	1.00
R7830:Cul9	UTSW	17	46,540,311 (GRCm38)	missense	probably benign	0.37
R7834:Cul9	UTSW	17	46,525,704 (GRCm38)	splice site	probably null
R8131:Cul9	UTSW	17	46,511,242 (GRCm38)	missense	probably damaging	1.00
R8192:Cul9	UTSW	17	46,538,347 (GRCm38)	missense	probably benign	0.01
R8231:Cul9	UTSW	17	46,520,501 (GRCm38)	missense	probably damaging	0.99
R8248:Cul9	UTSW	17	46,530,014 (GRCm38)	missense	probably damaging	0.99
R8504:Cul9	UTSW	17	46,503,580 (GRCm38)	missense	probably damaging	1.00
R8550:Cul9	UTSW	17	46,519,846 (GRCm38)	missense	probably damaging	1.00
R8716:Cul9	UTSW	17	46,527,914 (GRCm38)	missense	probably benign	0.28
R8769:Cul9	UTSW	17	46,521,902 (GRCm38)	missense	possibly damaging	0.85
R8893:Cul9	UTSW	17	46,500,849 (GRCm38)	small deletion	probably benign
R8904:Cul9	UTSW	17	46,520,501 (GRCm38)	missense	probably damaging	0.99
R8936:Cul9	UTSW	17	46,528,602 (GRCm38)	missense	possibly damaging	0.82
R8972:Cul9	UTSW	17	46,543,251 (GRCm38)	missense	probably damaging	1.00
R9003:Cul9	UTSW	17	46,525,075 (GRCm38)	missense	possibly damaging	0.78
R9012:Cul9	UTSW	17	46,543,521 (GRCm38)	missense	probably benign
R9056:Cul9	UTSW	17	46,543,770 (GRCm38)	missense	probably damaging	0.99
R9071:Cul9	UTSW	17	46,526,453 (GRCm38)	missense	probably benign
R9162:Cul9	UTSW	17	46,526,603 (GRCm38)	missense	probably benign	0.32
R9476:Cul9	UTSW	17	46,510,907 (GRCm38)	missense	probably damaging	1.00
R9526:Cul9	UTSW	17	46,530,100 (GRCm38)	missense	probably benign	0.41
R9563:Cul9	UTSW	17	46,509,971 (GRCm38)	missense	probably benign	0.01
R9568:Cul9	UTSW	17	46,520,118 (GRCm38)	missense	possibly damaging	0.56
R9610:Cul9	UTSW	17	46,519,897 (GRCm38)	missense	possibly damaging	0.96
R9611:Cul9	UTSW	17	46,519,897 (GRCm38)	missense	possibly damaging	0.96
R9705:Cul9	UTSW	17	46,543,300 (GRCm38)	missense	probably damaging	1.00
R9765:Cul9	UTSW	17	46,539,298 (GRCm38)	missense	probably benign	0.18
RF011:Cul9	UTSW	17	46,500,848 (GRCm38)	small insertion	probably benign
RF016:Cul9	UTSW	17	46,500,863 (GRCm38)	nonsense	probably null
RF026:Cul9	UTSW	17	46,500,869 (GRCm38)	nonsense	probably null
RF027:Cul9	UTSW	17	46,500,848 (GRCm38)	small insertion	probably benign
RF030:Cul9	UTSW	17	46,500,869 (GRCm38)	small insertion	probably benign
RF033:Cul9	UTSW	17	46,500,854 (GRCm38)	small insertion	probably benign
RF039:Cul9	UTSW	17	46,500,854 (GRCm38)	small insertion	probably benign
RF041:Cul9	UTSW	17	46,500,854 (GRCm38)	nonsense	probably null
RF042:Cul9	UTSW	17	46,540,615 (GRCm38)	frame shift	probably null
RF057:Cul9	UTSW	17	46,500,863 (GRCm38)	nonsense	probably null
Z1176:Cul9	UTSW	17	46,520,585 (GRCm38)	nonsense	probably null
Z1176:Cul9	UTSW	17	46,520,576 (GRCm38)	nonsense	probably null
Z1177:Cul9	UTSW	17	46,537,797 (GRCm38)	missense	probably benign	0.14

Predicted Primers

PCR Primer
(F):5'- TTTACAAAGAGCATTGTGGGAC -3'
(R):5'- ATCTCTGCCAGGGTTAGTACC -3'

Sequencing Primer
(F):5'- CGGTGCTTTGCGGGAGATAAC -3'
(R):5'- GGTTAGTACCCTCAGCCATG -3'

Posted On

2015-04-06